Canonical Allele Identifier: CA508989429
Gene: TNNI3 HGNC NCBI

Linked Data

dbSNP Id: rs1599909205
MyVariant Identifiers: chr19:g.55665497A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154129A>C , CM000681.2:g.55154129A>C GRCh38
NC_000019.9:g.55665497A>C , CM000681.1:g.55665497A>C GRCh37
NC_000019.8:g.60357309A>C NCBI36
NG_007866.2:g.8604T>G , LRG_432:g.8604T>G
NG_011829.2:g.110T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.450T>G MANE Select ENSP00000341838.5:p.Ser150=
ENST00000665070.1:c.483T>G ENSP00000499482.1:p.Ser161=
ENST00000344887.9:c.450T>G ENSP00000341838.5:p.Ser150=
ENST00000585806.5:n.449T>G
ENST00000586669.5:n.458T>G
ENST00000588882.1:c.375T>G ENSP00000466729.1:p.Ser125=
ENST00000589864.1:n.278T>G
NM_000363.4:c.450T>G , LRG_432t1:c.450T>G NP_000354.4:p.Ser150=
NM_000363.5:c.450T>G MANE Select NP_000354.4:p.Ser150=
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